Data / Drug companies / Oxaliplatin
Oxaliplatin: 16 companies and 42 products in the FDA NDC directory
Oxaliplatin is listed in the FDA National Drug Code Directory by 16 companies, with 42 products in commercial distribution. 42 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, solution; injection, powder, lyophilized, for solution; injection, solution, concentrate, and the newest product started marketing on January 15, 2026.
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- Companies listing it
- 16
- Products
- 42
- Generic (ANDA) products
- 42 (100.0%)
- Application numbers
- 13
- Routes
- Intravenous
- openFDA record search
- api.fda.gov
Companies that list oxaliplatin
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Meitheal Pharmaceuticals Inc. | 6 | injection, solution | Generic drugs (ANDA) | January 11, 2024 |
| Gland Pharma Limited | 5 | injection, solution; injection, powder, lyophilized, for solution | Generic drugs (ANDA) | November 6, 2017 |
| Qilu Pharmaceutical Co., Ltd. | 5 | injection, solution; injection, powder, lyophilized, for solution | Generic drugs (ANDA) | June 7, 2016 |
| NorthStar RxLLC | 4 | injection, solution | Generic drugs (ANDA) | January 11, 2024 |
| Sandoz Inc | 4 | injection, solution | Generic drugs (ANDA) | July 1, 2016 |
| Apotex Corp. | 2 | injection, solution | Generic drugs (ANDA) | April 23, 2024 |
| Baxter Healthcare Corporation | 2 | injection, solution | Generic drugs (ANDA) | February 19, 2018 |
| Camber Pharmaceuticals, Inc. | 2 | injection, solution, concentrate | Generic drugs (ANDA) | January 27, 2025 |
| Eugia US LLC | 2 | injection, solution | Generic drugs (ANDA) | September 21, 2017 |
| Fosun Pharma USA Inc. | 2 | injection, solution | Generic drugs (ANDA) | March 30, 2020 |
| Mylan Institutional LLC | 2 | injection, solution | Generic drugs (ANDA) | August 25, 2014 |
| Shandong New Time Pharmaceutical Co., Ltd. | 2 | injection, solution | Generic drugs (ANDA) | January 15, 2026 |
| Accord Healthcare Inc. | 1 | injection, solution, concentrate | Generic drugs (ANDA) | May 17, 2018 |
| BluePoint Laboratories | 1 | injection, solution | Generic drugs (ANDA) | December 9, 2020 |
| Hospira, Inc. | 1 | injection, solution, concentrate | Generic drugs (ANDA) | August 10, 2009 |
| Sagent Pharmaceuticals | 1 | injection, solution | Generic drugs (ANDA) | September 15, 2014 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, solution | 34 | 81% |
| Injection, powder, lyophilized, for solution | 4 | 9.5% |
| Injection, solution, concentrate | 4 | 9.5% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 42 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Platinum-based Drug | 42 |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.